A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4166n54



Internal ID22772061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20010432..21086140hg38UCSC Ensembl
chr15:20215685..21291469hg19UCSC Ensembl
chr15:18475699..19556128hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381075709
hg191075785
hg181080430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567227, nsv567169, nsv567315, nsv567238, nsv567157, nsv567160, nsv567276, nsv567278, nsv567229, nsv567288, nsv567171, nsv567247, nsv567299, nsv567282, nsv567170, nsv567257, nsv567239, nsv567156, nsv567154, nsv567290, nsv567168, nsv567275, nsv567272, nsv567162, nsv567309, nsv567173, nsv567298, nsv567222, nsv567172, nsv567289, nsv567274, nsv567182, nsv567262, nsv567277, nsv567305, nsv567230, nsv567180, nsv567273, nsv567304, nsv567271, nsv567183, nsv567179, nsv567270
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4166n54
Frequency
Sample Size17421
Observed Gain52
Observed Loss0
Observed Complex0
Frequencyn/a


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